The exploitation of thallium (Tl) resources through mining poses a significant threat to ecological systems and human health due to its high toxicity and ready assimilation by human body. We report the first assessment of the pollution, spatial distribution, source, and ecological-health risks of potentially toxic elements (PTEs) in Tl mining area of southwest Guizhou, China. Spatial distribution maps for PTEs were visualized by ArcGIS to identify their distribution trends. We use the enrichment factor (EF), correlation analysis, and principal component analysis to identify likely sources of seven PTEs mining area. The wider risk assessment was evaluated using the geoaccumulation index (Igₑₒ), potential ecological risk index (RI), human non-carcinogenic risk (HI), and carcinogenic risk (CR). The results revealed the PTEs content in the study area identifies direct mining, metal production, and domestic pollution sources. In addition, the distribution of PTEs was also affected by the topography, rain water leaching, and river dispersals. The main elements of concern are Tl and As, while Cd, Cr, Cu, Pb, and Zn do not show significant enrichment in the area despite associations with the ore deposit. Risk assessment identifies strong pollution and ecological risks and poses unacceptable human health risks to local residents, especially for children. The ecological risk in the study is identified to be predominantly from Tl (74.32%), followed by As (8.57%) and Cd (7.32%). The contribution of PTEs to the non-carcinogenic risk of humans in the study area is exclusively from As and Tl, while the carcinogenic risk is dominated by As, and the other elements pose no significant risk to human health.

In this study, a new ecological dam based on the microbial fuel cell principle (MFCED) was designed to remove pollutants from river sediments and water bodies. Sediment organics were better removed in the MFCED mode in comparison with the other two modes (ecological dam with open circuit (OCED) and ecological dam filled with gravel in cathode chamber (GMFCED)). The difference of nitrogen source in water had little effect on the removal of chemical oxygen demand (COD) (70–80%), while nitrate was more readily removed in the MFCED. The voltage curve and power curve were measured to understand the bioelectricity generation of MFCED. During the stable operation phase of MFCED, the voltage was stabilized between 0.09–0.15 V. The results of high-throughput sequencing indicated that the anode and cathode diversities of MFCED were more than the other systems, and the species diversity of the anode was more than that of the cathode in the MFCED. Graphical abstract

Lung cancer as one of the major causes of cancer mortality has been demonstrated to be closely related to the ambient atmospheric environment, but little has been done in the synthetic evaluation of the linkage between cancer mortality and combined impact of ambient air pollution and meteorological conditions. The present study determined the environmental suitability for female lung cancer mortality associated with air contaminants and meteorological variables. A novel fuzzy matter–element method was applied to identify the spatial distribution and regions for the environmental suitability for the female lung cancer mortality across China in 2013. The membership functions between the cancer mortality and 6 environmental factors, including PM₂.₅, NO₂, SO₂, PM₁₀, the annual mean wind speed, and mean temperature, were generated and the weights of each of the environmental factors were established by the maximum entropy (MaxEnt) model. We categorized the environmental suitability combined with GIS spatial analysis into three zones, including low-suitable, medium-suitable, and high-suitable region where the cancer mortality ranging from low to high rate was identified. These three zones were quantified by the MaxEnt model taking different air pollutants and meteorological variables into consideration. We identified that NO₂ was a most significant factor among the 6 environmental factors with the weight of 24.88%, followed by the annual mean wind speed, SO₂, and PM₂.₅. The high-suitable area, mainly in the North China Plain which is a most heavily contaminated region by air pollution in China, covers 1.6195 million square kilometers, accounting for 17.85% of the total area investigated in this study. Identification of the impact of various environmental factors on cancer mortality in the different suitable area provides a scientific basis for the environmental management, risk assessment, and lung cancer control.

An electrokinetic batch treatment scheme was investigated combining sequential electrocoagulation (EC) and chemical coagulation treatment (CC) processes. Synthetic and microbrewery wastewaters were tested in this investigation. The generated results demonstrated the capacity for the integration of EC-CC to effectively remove phosphorus contamination from wastewater under varying operating conditions. The effect of several operational parameters such as current density, conductivity, nutrient loading, and electrolysis time were investigated. The results showed that increased salinity can significantly accelerate the removal of phosphorous during EC treatment with 84.2% and 92.4% removal found for the applied power of 5 and 10 W, respectively. The addition of a sequential chemical coagulant stage following treatment by EC demonstrated the potential for an integrated EC-CC system to lower energy consumption while maintaining effective nutrient removal capabilities. Removal of phosphorous at 95% and 98% was achieved in just 10 min of EC treatment coupled with the addition of 15 mg/L aluminum sulfate. The estimated power consumption over a 10-min period was found to be 0.28 Kwh/m³ with a dissolution rate of 0.28 g/cm² min held at a constant current density. The experimental anode dissolution rate for the synthetic wastewater ranged between 0.13 and 0.24 g/cm² min encompassing all salinity levels. The anode dissolution rate increased during treatment of microbrewery wastewater with 0.67 g/cm² min for 10 W EC treatment. This was attributed to the increase in current density and nutrient loading resulting in increased energy consumption and electrode passivation.

Much of the existing research analyses on emissions and climate policy are dominantly based on emissions data provided by production-based accounting (PBA) system. However, PBA provides an incomplete picture of driving forces behind these emission changes and impact of global trade on emissions, simply by neglecting the environmental impacts of consumption. To remedy this problem, several studies propose to consider national emissions calculated by consumption-based accounting (CBA) systems in greenhouse gas (GHG) assessments for progress and comparisons among the countries. In this article, we question the relevance of PBA’s dominance. To this end, we, firstly, try to assess and compare PBA with CBA adopted in greenhouse gas emissions accounting systems in climate change debates on several issues and to discuss the policy implications of the choice of approach. Secondly, we investigate the convergence patterns in production-based and consumption-based emissions in 35 Annex B countries for the period between 1990 and 2015. This study, for the first time, puts all these arguments together and discusses possible outcomes of convergence analysis by employing both the production- and consumption-based CO₂ per capita emissions data. The empirical results found some important conclusions which challenge most of the existing CO₂ convergence studies.

Bio-mix is a fuel derived from the raw mixture of different non-edible oils to enhance the saturation level. In this study, raw oil mixture was transesterified to form bio-mix methyl ester (BMME). Fuel properties of BMME was measured and results showed that saturated fatty acids (SFA), cetane number (CN), and oxidation stability (OS) were increased, whereas density, viscosity, HHV, flash point, iodine number, and acid number were decreased for BMME as compared to individual biodiesels. Brake specific energy consumption (BSEC) of BMME was higher than diesel fuel but similar to individual biodiesel, while brake thermal efficiency (BTE) was lower than diesel fuel but higher than the individual biodiesel. (NOₓ) and CO₂ emission of BMME was found lower (approximately 20%); meanwhile, smoke opacity and CO emission biodiesel increased compared to diesel fuel, whereas (HC) emission of BMME was lower at low load condition but it is increased at high load. Bio-mix fuel could be the good replacement of diesel fuel.

The aim of this work is to evaluate the application of a steel waste, basic oxygen furnace sludge (BOFS), rich in iron, to treat water contaminated with elevated arsenic and sulfate concentrations. In the first step, three doses (10, 60, and 80 g L⁻¹) of BOFS were tested to investigate the removal of As(III) and As(V) (67 mg L⁻¹) and sulfate (3700 mg L⁻¹) separately from an aqueous solution. In the second step, the efficacies of BOFS (10 g L⁻¹) and commercial ZVI (5 g L⁻¹) were compared to simultaneously remove arsenic and sulfate. The pH of the feed solution was adjusted to 2.5 and monitored during the experiment. The use of BOFS achieved arsenic removal up to 92% and sulfate removal of nearly 40% after 72 h of contact time. Use of BOFS also increased the solution pH to 12. Similar removal levels were achieved with both BOFS and ZVI. These results confirm the potential application of BOFS to remove high arsenic and sulfate concentrations from acidic solutions. The data obtained here should be used as a basis for further studies on the remediation of acid mine drainage with high concentrations of arsenic and sulfate using an abundant and low-cost steel waste.

Calcium ion-incorporated hydrous iron(III) oxide (CIHIO) samples have been prepared aiming investigation of efficiency enhancement on arsenic and fluoride adsorption of hydrous iron(III) oxide (HIO). Characterization of the optimized product with various analytical tools confirms that CIHIO is microcrystalline and mesoporous (pore width, 26.97 Å; pore diameter, 27.742 Å with pore volume 0.18 cm³ g⁻¹) material. Increase of the BET surface area (> 60%) of CIHIO (269.61 m² g⁻¹) relative to HIO (165.6 m² g⁻¹) is noticeable. CIHIO particles are estimated to be ~ 50 nm from AFM and TEM analyses. Although the pH optimized for arsenite and fluoride adsorptions are different, the efficiencies of CIHIO towards their adsorption are very good at pH 6.5 (pHzₚc). The adsorption kinetics and equilibrium data of either tested species agree well, respectively, with pseudo-second order model and Langmuir monolayer adsorption phenomenon. Langmuir capacities (mg g⁻¹at 303 K) estimated are 29.07 and 25.57, respectively, for arsenite and fluoride. The spontaneity of adsorption reactions (ΔG⁰ = − 18.02 to − 20.12 kJ mol⁻¹ for arsenite; − 0.2523 to − 3.352 kJ mol⁻¹ for fluoride) are the consequence of entropy parameter. The phosphate ion (1 mM) compared to others influenced adversely the arsenite and/or fluoride adsorption reactions. CIHIO (2.0 g L⁻¹) is capable to abstract arsenite or fluoride above 90% from their solution (0 to 5.0 mg L⁻¹). Mechanism assessment revealed that the adsorption of arsenite occurs via chelation, while of fluoride occurs with ion-exchange.

Specific and sensitive detection of fecal microbes in potable water is essential for ensuring the safety of water supplies. To this end, because conventional culture-based methods typically require at least 24 h to detect fecal bacteria, rapid and simple microbiological detection methods are considered necessary. Fluorescence in situ hybridization (FISH) is a useful culture-independent technique for selectively and rapidly detecting target bacteria using fluorescently labeled probes that hybridize with intracellular ribosomal RNA. However, typical FISH assays are relatively complicated to perform, making FISH unsuitable for routine tests. In this study, we developed an “in liquid-fluorescence in situ hybridization” assay (liq-FISH) to enumerate Escherichia coli cells, indicator of fecal contamination, rapidly. The assay performs the entire in situ hybridization procedure in liquid and requires only two simple steps—addition of fixative followed by the addition of fluorescent probe. Important processes in FISH, fixation and hybridization, were optimized, and then specificity of the optimized liq-FISH procedure was confirmed by E. coli and other eight gammaproteobacterial species. The findings showed that only E. coli cells fluoresced under a fluorescence microscope; however, filtration process is required to observe and count hybridized cells by fluorescence microscopy. For simple and semi-automated counting following liq-FISH, our developed microscope-based microfluidic counting system was applied. Hybridized cells were injected into a microfluidic device, which permitted the detection and enumeration of E. coli cells flowing through the microchannel (width: 100 μm, depth: 15 μm). The obtained results were compared with those obtained by conventional fluorescence microscopy, and results showed the similarity (r = 0.908). E. coli cells could be counted within 5 h (filtration for concentration of low numbers of E. coli cells (if necessary): 0.5 h, fixation of cells: 2 h, in situ hybridization: 2 h, counting: 0.5 h), and this method would be useful for rapidly quantifying E. coli cells in potable water.

Sulfur-doped activated carbons (SACs) with high sulfur content and large specific surface area were synthesized from polythiophene for acetone removal. The sulfur content of carbons (3.10–8.43 at.%) could be tunable by adjusting the activation temperature. The BET surface area and pore volume of the obtained samples were 916–2020 m² g⁻¹ and 0.678–1.100 cm³ g⁻¹, with a significant proportion of microporosity (up to 84% and 72% for BET surface area and pore volume, respectively). The resulting SACs show a superior acetone adsorption capacity (i.e., 716.4 mg g⁻¹ at 15 °C and 705 mg g⁻¹ at 25 °C for SAC700). In terms of the adsorption behavior of acetone on the activated carbons, compared to the Langmuir model, the Langmuir-Freundlich model showed better agreement with the adsorption amount. The results reveal that the surface area and micropore volume are the key factors for acetone adsorption, while the sulfur-doped functional groups, especially oxidized sulfur functional groups, can enhance the acetone adsorption capacity at a certain low pressure. Temperature programmed desorption (TPD) experiments were performed to get desorption activation energy of acetone on SAC samples, and the results ranged from 23.54 to 38.71 kJ mol⁻¹. The results of the molecular simulation show that the introduction of sulfur element can increase the binding energy between acetone molecule and carbon surface, and the tri-oxidized sulfur (sulfonic acid) functional group has the highest binding energy of − 0.4765 eV. Graphical abstract